{
  "id": 20282,
  "label": "keratosis pilaris",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0021036",
  "properties": {
    "xrefs": [
      "MEDGEN:82664",
      "NCIT:C124070",
      "SCTID:5132005",
      "UMLS:C0263383",
      "icd11.foundation:1614890502"
    ],
    "synonyms": [
      "KP"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "A form of dry skin characterized by hair follicles plugged by scale."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 6820,
      "label": "skin disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4198
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:37",
          "EFO:0000701",
          "ICD9:702",
          "ICD9:702.8",
          "ICD9:709.8",
          "MEDGEN:20777",
          "MESH:D012871",
          "NANDO:2100281",
          "NCIT:C3371",
          "SCTID:95320005",
          "UMLS:C0037274"
        ],
        "synonyms": [
          "cutaneous disorder",
          "disease of zone of skin",
          "disease or disorder of zone of skin",
          "disorder of skin",
          "disorder of zone of skin",
          "skin diseases and manifestations",
          "skin disorder",
          "zone of skin disease",
          "zone of skin disease or disorder",
          "dermatosis",
          "genodermatosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Any deviation from the normal structure or function of the skin or subcutaneous tissue that is manifested by a characteristic set of symptoms and signs."
      },
      "child_count": 72,
      "reference_id": "MONDO:0005093"
    }
  ],
  "children": [
    {
      "id": 18791,
      "label": "keratosis pilaris atrophicans",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19129,
        20282,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080751",
          "GARD:0018694",
          "ICD9:757.39",
          "MEDGEN:75520",
          "MESH:C537412",
          "OMIM:604093",
          "Orphanet:498",
          "SCTID:400059005",
          "UMLS:C0263428",
          "icd11.foundation:273325594"
        ],
        "synonyms": [
          "keratosis pilaris atrophicans",
          "Atrophodermia reticulata",
          "Atrophodermia reticulata symmetrica faciei",
          "Atrophodermia vermiculata",
          "KPA",
          "amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2",
          "burnett Schwartz Berberian syndrome",
          "folliculitis ulerythematosa",
          "folliculitis ulerythematosa reticulata",
          "honeycomb atrophy",
          "keratosis pilaris",
          "keratosis pilaris atrophicans facies",
          "ulerythema ophryogenes",
          "ulerythema ophryogenes with multiple congenital anomalies",
          "ulerythema ophryogenesis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An uncommon form of keratosis pilaris in which there are scar-like follicular depressions and loss of hair."
      },
      "child_count": 12,
      "reference_id": "MONDO:0018855"
    }
  ],
  "roots": [
    {
      "id": 6820,
      "label": "skin disorder"
    }
  ]
}